JP3865113B2 - Cleaning gas and etching gas - Google Patents

Cleaning gas and etching gas Download PDF

Info

Publication number
JP3865113B2
JP3865113B2 JP2000207473A JP2000207473A JP3865113B2 JP 3865113 B2 JP3865113 B2 JP 3865113B2 JP 2000207473 A JP2000207473 A JP 2000207473A JP 2000207473 A JP2000207473 A JP 2000207473A JP 3865113 B2 JP3865113 B2 JP 3865113B2
Authority
JP
Japan
Prior art keywords
gas
silicon
coochf
compound
etching
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP2000207473A
Other languages
Japanese (ja)
Other versions
JP2002020796A (en
Inventor
澤 銀次郎 冨
井 有 規 三
江 功 也 深
屋 章 関
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kanto Denka Kyogyo Co.,Ltd.
Daikin Industries Ltd
Renesas Technology Corp
Showa Denko KK
Canon Anelva Corp
Toshiba Corp
Tokyo Electron Ltd
Fujitsu Ltd
Panasonic Corp
Hitachi Kokusai Electric Inc
National Institute of Advanced Industrial Science and Technology AIST
Sanyo Electric Co Ltd
Sony Corp
Ulvac Inc
AGC Inc
Panasonic Holdings Corp
Original Assignee
Kanto Denka Kyogyo Co.,Ltd.
Daikin Industries Ltd
Renesas Technology Corp
Asahi Glass Co Ltd
Showa Denko KK
Canon Anelva Corp
Toshiba Corp
Tokyo Electron Ltd
Fujitsu Ltd
Panasonic Corp
Hitachi Kokusai Electric Inc
National Institute of Advanced Industrial Science and Technology AIST
Sanyo Electric Co Ltd
Sony Corp
Ulvac Inc
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kanto Denka Kyogyo Co.,Ltd., Daikin Industries Ltd, Renesas Technology Corp, Asahi Glass Co Ltd, Showa Denko KK, Canon Anelva Corp, Toshiba Corp, Tokyo Electron Ltd, Fujitsu Ltd, Panasonic Corp, Hitachi Kokusai Electric Inc, National Institute of Advanced Industrial Science and Technology AIST, Sanyo Electric Co Ltd, Sony Corp, Ulvac Inc, Matsushita Electric Industrial Co Ltd filed Critical Kanto Denka Kyogyo Co.,Ltd.
Priority to JP2000207473A priority Critical patent/JP3865113B2/en
Priority to PCT/JP2001/005761 priority patent/WO2002005338A1/en
Publication of JP2002020796A publication Critical patent/JP2002020796A/en
Application granted granted Critical
Publication of JP3865113B2 publication Critical patent/JP3865113B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/4401Means for minimising impurities, e.g. dust, moisture or residual gas, in the reaction chamber
    • C23C16/4405Cleaning of reactor or parts inside the reactor by using reactive gases
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00Capture or disposal of greenhouse gases
    • Y02C20/30Capture or disposal of greenhouse gases of perfluorocarbons [PFC], hydrofluorocarbons [HFC] or sulfur hexafluoride [SF6]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Drying Of Semiconductors (AREA)
  • Detergent Compositions (AREA)
  • Physical Vapour Deposition (AREA)
  • Chemical Vapour Deposition (AREA)

Description

【0001】
【発明の技術分野】
本発明は、チャンバークリーニング用ガス及びエッチングガスに関する。さらに詳しくは、地球温暖化への寄与の小さいフッ素系化合物からなる半導体基板製造に好適なCVD装置等のチャンバークリーニング用ガス及びエッチングガスに関する。
【0002】
【発明の技術的背景】
従来、半導体製造等における薄膜デバイスの製造プロセス等においては、CVD法等を用いて、種々の薄膜、厚膜の形成が行われている。このような半導体用の薄膜を形成する際、膜を成膜させるべき目的物以外の反応容器内壁、目的物を担持する冶具、配管等にも薄膜原料と同じものが付着してしまう。このような付着物は、半導体製品への微粒子の混入原因となり、高品質な薄膜製造が困難となるとともに製品の歩留りの低下を招くこともあり、随時除去することが必要であり、従来、人手あるいはクリーニングガスなどにより付着物の除去が行われていた。
【0003】
また、半導体等においては、半導体回路を構成する各種の薄膜材料に回路パターンを形成するため、薄膜材料を部分的に除去するガスエッチングが用いられていた。
このようなクリーニングガスあるいはエッチングガスに求められる基本的な性能は、クリーニングガスの場合はクリーニング速度が速いこと、エッチングガスの場合は、目的物に対するエッチング速度が速いこと、選択性が高いことなどである。また、両者に共通して、排ガスの処理が容易であること、取り扱いが容易であること、さらに地球環境にやさしいこと等が挙げられる。
【0004】
従来、このような付着物のクリーニングガスあるいは薄膜のエッチングガスとしては、CF4、C26、SF6、NF3などのパーフルオロ化合物が半導体の製造工程で大量に用いられていた。
しかしながら、これらのフッ素系ガスは、大気中で寿命の長い安定な化合物であり、また、エッチング後の排ガス処理が困難で、その処理コストが高いという問題点があった。また、地球温暖化係数(積分期間100年値)が、CF4は6500、C26は9200、SF6は23900、NF3は8000と極めて大きく、環境への悪影響が懸念されるという問題点もあった。このため、地球温暖化係数が小さく、しかも半導体のケイ素系化合物に対するクリーニング性能、あるいはケイ素系化合物膜に対するエッチング性能に優れた代替ガスの開発が求められていた。
【0005】
そこで本願発明者らは、上記問題を解決すべく鋭意研究し、特定のフッ素系エステル化合物が、大気寿命が短く、地球温暖化に与える影響が小さく、かつ取扱いが容易であり、クリーニング後あるいはエッチング後の排ガス処理がしやすく、ケイ素系化合物膜に対し優れたクリーニング性能及びエッチング性能を有していることを見出し、本願発明を完成するに至った。
【0006】
【発明の目的】
本発明は、地球温暖化の影響が小さく、しかも取扱いが容易であり、排ガス処理性に優れるとともに、ケイ素系化合物に対するクリーニング性能あるいはケイ素系化合物膜に対するクリーニング性能に優れ、半導体製造に好適なCVD装置等のチャンバークリーニング用ガス及びエッチングガスを提供することを目的としている。
【0007】
【発明の概要】
本発明に係るチャンバークリーニング用ガスは、CF3COOCHF2、C25COOCHF2、CF3COOC25及びC25COOC25からなる群から選ばれる少なくとも1種のフッ素系化合物であることを特徴としている。また、前記フッ素系化合物は、CF3COOCHF2またはC25COOCHF2から選ばれる少なくとも1種であることが好ましい。前記チャンバークリーニング用ガスは、CVD装置チャンバーのクリーニングガスであることが好ましい。前記チャンバークリーニング用ガスは、ケイ素系化合物からなる付着物のクリーニング用ガスであることが好ましい。また、前記ケイ素系化合物は、(1)ケイ素からなる化合物、(2)酸素、窒素、フッ素または炭素のうちの少なくとも1種と、ケイ素とからなる化合物、または(3)高融点金属シリサイトからなる化合物のうちの少なくとも1種であることが好ましい。
【0008】
本発明に係るケイ素系化合物膜用エッチングガスは、CF3COOCHF2、C25COOCHF2、CF3COOC25及びC25COOC25からなる群から選ばれる少なくとも1種のフッ素系化合物であることを特徴としている。また、前記ケイ素系化合物膜は、(1)ケイ素からなる膜、(2)酸素、窒素、フッ素または炭素のうちの少なくとも1種と、ケイ素とからなる膜、または(3)高融点金属シリサイト膜のうちの少なくとも1種であることが好ましい。
【0009】
さらに、前記フッ素系化合物は、CF3COOCHF2またはC25COOCHF2から選ばれる少なくとも1種であることが好ましい。
【0010】
【発明の具体的説明】
本発明に係るケイ素系化合物膜用チャンバークリーニング用ガス及びエッチングガスは、特定のフッ素系エステル化合物である。以下にそれぞれについて詳細に説明する。
[チャンバークリーニング用ガス]
本発明に係る、チャンバークリーニング用ガスは、CF3COOCHF2、C25COOCHF2、CF3COOC25及びC25COOC25からなる群から選ばれる少なくとも1種のフッ素系化合物である。
【0011】
このうち、本発明においては、好ましくはCF3COOCHF2及び/またはC25COOCHF2をチャンバークリーニング用ガスとして用いることが望ましい。
なお、本明細書においてチャンバークリーニングとは、CVD装置等の半導体製造装置内のチャンバー壁あるいは冶具、配管等に付着した付着物の除去を意味している。
【0012】
これらのフッ素系化合物は1種単独で、または2種以上を混合して、CVD装置等のチャンバークリーニング用ガスとして用いることができる。
このような本発明に係るチャンバークリーニング用ガスは、エステル結合を有し、大気中での寿命が極めて短く地球温暖化への寄与度が小さいことから、未反応の前記チャンバークリーニング用ガスの放出による環境影響を小さく抑えることができる。また、既存のパーフルオロ化合物の大気寿命(たとえば、CF4は50000年、C26は10000年、C38は7000年、SF6は3200年、NF3は740年である。)に対し、本発明に係るチャンバークリーニング用ガスの大気寿命は、数年以内と推定される。さらに、本発明に係るチャンバークリーニング用ガスは、排ガス処理が容易である。
【0013】
またさらに、前記フッ素系化合物は、比較的沸点が低く、半導体製造条件下では気体であることから、チャンバークリーニングにおける取扱いが容易である。このようなフッ素系化合物によるチャンバークリーニングの目的化合物としては、CVD法等により、CVDチャンバー壁あるいはCVD装置の冶具等に付着した、前記ケイ素系化合物からなる付着物が挙げられる。このようなケイ素系化合物の付着物としては、たとえば、
(1)ケイ素からなる化合物、
(2)酸素、窒素、フッ素または炭素のうちの少なくとも1種と、ケイ素とからなる化合物、または
(3)高融点金属シリサイトからなる化合物
などのうちの少なくとも1種が挙げられ、より具体的には、たとえば、Si、SiO2、Si34、WSi等の高融点金属シリサイトなどが挙げられる。
【0014】
また、本発明に係るクリーニングガスは、適宜他のガスを混合して用いることができる。このような他のガスとしては、たとえば、He、Ne、Ar、O2などが挙げられる。このような他のガスの配合量は特に限定されず、CVD装置等のチャンバーに付着した付着物の量、厚みなどに対応して決定することができる。
【0015】
これらのフッ素系化合物の製造方法は、特に限定されない。たとえば、CF3COOCHF2は、次の方法により収率良く製造することができる。
(CH3COO)2Hg + 2CF2HI → 2CH3COOCHF2 + HgI反応温度は、20〜80℃、好ましくは40〜70℃程度であり、反応時間は、2〜30時間、好ましくは10〜20時間程度であることが望ましい。前記反応は、無溶媒で行うことができる。
【0016】
また、たとえばCF3COOC25は、CH3COOC25に、低温(−196〜0℃)にて、F2ガスを直接作用させることにより得ることができる。
本発明に係るチャンバークリーニング用ガスを用いるチャンバーの材料は特に限定されず、公知の材料が挙げられる。このようなチャンバーの材料としては、たとえば、ステンレス、アルミニウム、あるいはこれらの合金などが挙げられる。 本発明に係るチャンバークリーニング用ガスは、このようなチャンバーに対しては腐食等の作用を及ぼすことが少なく、チャンバーに付着した前記付着物を選択的かつ迅速に除去することができる。
【0017】
このような本発明に係るフッ素系化合物を用いて、チャンバー内のケイ素系化合物等からなる付着物をクリーニングするには、公知の方法が採用でき、たとえば、プラズマクリーニング、リモートプラズマクリーニング、マイクロ波クリーニングなどの各種ドライクリーニング法が適用できる。
このような本発明に係るチャンバークリーニング用ガスによれば、ケイ素系化合物を除去することが可能である。
[ケイ素系化合物膜用エッチングガス]
本発明に係る、ケイ素系化合物膜用エッチングガスは、CF3COOCHF2、C25COOCHF2、CF3COOC25及びC25COOC25からなる群から選ばれる少なくとも1種のフッ素系化合物である。
【0018】
このうち、本発明においては、好ましくはCF3COOCHF2及び/またはC25COOCHF2をケイ素系化合物膜のエッチングガスとして用いることが望ましい。
これらのフッ素系化合物は1種単独で、または2種以上を混合して、エッチングに用いることができる。
【0019】
また、本発明に係るエッチングガスは、He、Ne、Ar、H2、N2、O2などの単体ガス、CH4、C26、NH3などの化合物ガスを適宜混合して用いることができる。このような他のガスの配合量は特に限定されず、エッチングの対象物であるケイ素系化合物膜の厚み、量などに対応して決定することができる。
エッチングの目的化合物としては、ケイ素系化合物からなる薄膜等が挙げられる。このようなケイ素系化合物膜としては、たとえば、
(1)ケイ素からなる膜、
(2)酸素、窒素、フッ素または炭素のうちの少なくとも1種と、ケイ素とからなる膜、または
(3)高融点金属シリサイト膜
などのうちの少なくとも1種が挙げられる。
【0020】
より具体的には、たとえば、Si膜、SiO2膜、Si34膜、WSi膜等の高融点金属シリサイト膜などが挙げられる。
このようなケイ素系化合物膜を、本発明に係るフッ素系化合物によりエッチングする方法は、公知の方法が採用でき、たとえば、プラズマエッチング、反応性イオンエッチング、マイクロ波エッチングなどの各種ドライエッチング法が適用できる。また、ケイ素系化合物膜のエッチング条件は、公知のエッチング条件を採用できる。
【0021】
このような本発明に係るエッチングガスは、エステル結合を有するため大気中で容易に加水分解し、大気寿命が短いことから地球温暖化への寄与度が小さく、未反応の前記エッチングガスの放出における環境影響を小さく抑えることができ、また、排ガス処理も容易である。
【0022】
【発明の効果】
本発明に係るチャンバークリーニング用ガスは、地球温暖化への寄与度が小さいことから、未反応の前記チャンバークリーニング用ガスの放出による環境影響を小さく抑えることができるとともに、排ガス処理が容易である。またこのチャンバークリーニング用ガスは、既存ガスに匹敵するクリーニング速度を有している。
【0023】
本発明に係るケイ素系化合物膜用エッチングガスは、地球温暖化寄与度が小さいことから、未反応のエッチングガスの放出による環境影響を低く抑えることができるとともに、排ガス処理が容易である。また、ケイ素系化合物の除去を効率的に、しかも半導体パターンの寸法精度を高精度に保ちながらエッチングが可能であり、既存ガスに匹敵するエッチング性能を有している。
【0024】
【実施例】
以下、実施例に基づいて本発明をより詳細に説明するが、これらの実施例により本発明は限定されるものではない。
【0025】
【調製例1】
[CF3COOCHF2の合成]
容器内を窒素で置換、乾燥した25mlのSUS−316製の反応容器に、(CF3COO)2Hgを2.2g(10mmol)を装入し、反応容器内を減圧した後、反応容器を液体窒素で冷却し、CF2HIを220ml(9.15mmol)加えた。次いで、反応容器を50℃に昇温し、この温度で15.5時間反応させた。
【0026】
得られた化合物(沸点19℃)をガスクロマトグラフィー及びFT−IRで分析し、得られた化合物はCF3COOCHF2であることを確認した。収率は、99%であった。
【0027】
【実施例1】
[チャンバークリーニング]
調製例1で合成したCF3COOCHF2を35%、酸素を65%含有する混合ガスを用いて、圧力110Pa、入力Rf電力290W、トータルガス流量60sccmの条件下で、SiO2膜を堆積したシリコンウェハーをCVDチャンバー内に置いてSiO2膜をクリーニングした。
【0028】
上記条件下で2分間クリーニングしたところ、クリーニング速度は540Å/minであった。
【0029】
【実施例2】
[チャンバークリーニング]
調製例1で合成したCF3COOCHF2を25%、酸素を75%含有する混合ガスを用いて、圧力110Pa、入力Rf電力290W、トータルガス流量60sccmの条件下で、Si34膜を堆積したシリコンウェハーをCVDチャンバー内に置いてSi34膜をクリーニングした。
【0030】
上記条件下で2分間クリーニングしたところ、クリーニング速度は4850Å/minであった。
【0031】
【実施例3】
[エッチング]
調製例1で合成したCF3COOCHF2を45%、酸素を60%含有する混合ガスを用いて、圧力110Pa、入力Rf電力300W、トータルガス流量60sccmの条件下で、Si34膜、SiO2膜をそれぞれ堆積したシリコンウェハーをエッチングして、Si34膜とSiO2膜の選択比(Si34膜のエッチング速度/SiO2膜のエッチング速度)を求めたところ、選択比は、17倍であった。
【0032】
【比較例1】
[チャンバークリーニング]
26を35%、酸素を65%含有する混合ガスを用いて、圧力110Pa、入力Rf電力290W、トータルガス流量60sccmの条件下で、SiO2膜を堆積したシリコンウェハーをCVDチャンバー内に置いてSiO2膜をクリーニングした。
【0033】
上記条件下で2分間クリーニングしたところ、クリーニング速度は630Å/minであった。
なお、C26は地球温暖化作用が大きいため、同作用の小さいクリーニングガスへの代替が求められているガスである。
[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a chamber cleaning gas and an etching gas. More specifically, the present invention relates to a chamber cleaning gas and an etching gas such as a CVD apparatus suitable for manufacturing a semiconductor substrate made of a fluorine-based compound that has a small contribution to global warming.
[0002]
TECHNICAL BACKGROUND OF THE INVENTION
2. Description of the Related Art Conventionally, in a thin film device manufacturing process in semiconductor manufacturing or the like, various thin films and thick films are formed using a CVD method or the like. When such a thin film for a semiconductor is formed, the same material as the thin film raw material adheres to the inner wall of the reaction vessel other than the target object on which the film is to be formed, the jig carrying the target object, the piping, and the like. Such deposits cause contamination of semiconductor products with fine particles, which makes it difficult to produce high-quality thin films and may reduce product yield. Alternatively, deposits have been removed with a cleaning gas or the like.
[0003]
In semiconductors and the like, gas etching for partially removing the thin film material has been used to form circuit patterns on various thin film materials constituting the semiconductor circuit.
The basic performance required for such a cleaning gas or etching gas is that the cleaning speed is high in the case of the cleaning gas, the etching speed with respect to the target is high in the case of the etching gas, and the selectivity is high. is there. Further, in common with both, it is easy to treat exhaust gas, easy to handle, and friendly to the global environment.
[0004]
Conventionally, perfluoro compounds such as CF 4 , C 2 F 6 , SF 6 , and NF 3 have been used in large amounts in the semiconductor manufacturing process as cleaning gases for such deposits or etching gases for thin films.
However, these fluorine-based gases are stable compounds having a long life in the atmosphere, and there are problems in that exhaust gas treatment after etching is difficult and the treatment cost is high. In addition, the global warming potential (integral period 100-year value) is as large as 6500 for CF 4 , 9200 for C 2 F 6 , 23900 for SF 6 and 8000 for NF 3. There was also a point. For this reason, there has been a demand for the development of an alternative gas that has a low global warming potential and that is excellent in cleaning performance of silicon based semiconductor compounds or etching performance of silicon based compound films.
[0005]
Therefore, the inventors of the present application have made extensive studies to solve the above-mentioned problems, and the specific fluorine-based ester compound has a short atmospheric life, has a small effect on global warming, is easy to handle, and after cleaning or etching. The inventors have found that the later exhaust gas treatment is easy and that the silicon compound film has excellent cleaning performance and etching performance, and the present invention has been completed.
[0006]
OBJECT OF THE INVENTION
The present invention is a CVD apparatus that is less affected by global warming, is easy to handle, has excellent exhaust gas treatment properties, has excellent cleaning performance for silicon compounds, or cleaning performance for silicon compound films, and is suitable for semiconductor manufacturing It is an object to provide a chamber cleaning gas and an etching gas.
[0007]
SUMMARY OF THE INVENTION
The chamber cleaning gas according to the present invention includes at least one fluorine-based compound selected from the group consisting of CF 3 COOCHF 2 , C 2 F 5 COOCHF 2 , CF 3 COOC 2 F 5 and C 2 F 5 COOC 2 F 5 . It is characterized by being. Further, the fluorine compound is preferably at least one selected from CF 3 COOCHF 2 or C 2 F 5 COOCHF 2. The chamber cleaning gas is preferably a cleaning gas for a CVD apparatus chamber. The chamber cleaning gas is preferably a cleaning gas for deposits made of a silicon compound. In addition, the silicon-based compound includes (1) a compound composed of silicon, (2) a compound composed of at least one of oxygen, nitrogen, fluorine, and carbon and silicon, or (3) a refractory metal silicite. It is preferable that it is at least 1 type of the compound which becomes.
[0008]
The etching gas for a silicon-based compound film according to the present invention is at least one selected from the group consisting of CF 3 COOCHF 2 , C 2 F 5 COOCHF 2 , CF 3 COOC 2 F 5 and C 2 F 5 COOC 2 F 5 . It is a fluorine compound. The silicon-based compound film may be (1) a film made of silicon, (2) a film made of silicon and at least one of oxygen, nitrogen, fluorine or carbon, or (3) a refractory metal silicite. It is preferably at least one of the membranes.
[0009]
Furthermore, the fluorine-based compound is preferably at least one selected from CF 3 COOCHF 2 or C 2 F 5 COOCHF 2 .
[0010]
DETAILED DESCRIPTION OF THE INVENTION
The silicon-based compound film chamber cleaning gas and the etching gas according to the present invention are specific fluorine-based ester compounds. Each will be described in detail below.
[Gas for chamber cleaning]
The chamber cleaning gas according to the present invention is at least one fluorine-based material selected from the group consisting of CF 3 COOCHF 2 , C 2 F 5 COOCHF 2 , CF 3 COOC 2 F 5 and C 2 F 5 COOC 2 F 5. A compound.
[0011]
Among these, in the present invention, it is preferable to use CF 3 COOCHF 2 and / or C 2 F 5 COOCHF 2 as the chamber cleaning gas.
In this specification, chamber cleaning means removal of deposits attached to a chamber wall, jig, piping, or the like in a semiconductor manufacturing apparatus such as a CVD apparatus.
[0012]
These fluorine compounds can be used alone or in combination of two or more as a chamber cleaning gas for a CVD apparatus or the like.
Such a chamber cleaning gas according to the present invention has an ester bond and has a very short lifetime in the atmosphere and a small contribution to global warming. Environmental impact can be kept small. In addition, the atmospheric lifetime of existing perfluoro compounds (for example, CF 4 is 50,000 years, C 2 F 6 is 10,000 years, C 3 F 8 is 7000 years, SF 6 is 3200 years, and NF 3 is 740 years). On the other hand, the atmospheric lifetime of the chamber cleaning gas according to the present invention is estimated to be within several years. Further, the chamber cleaning gas according to the present invention can be easily treated with an exhaust gas.
[0013]
Furthermore, since the fluorine-based compound has a relatively low boiling point and is a gas under semiconductor manufacturing conditions, it is easy to handle in chamber cleaning. Examples of the target compound for chamber cleaning with such a fluorine-based compound include deposits made of the silicon-based compound attached to a CVD chamber wall or a jig of a CVD apparatus by a CVD method or the like. Examples of such silicon compound deposits include:
(1) a compound comprising silicon,
(2) At least one of oxygen, nitrogen, fluorine, or carbon and a compound composed of silicon, or (3) a compound composed of refractory metal silicite, and the like. Examples thereof include refractory metal silicite such as Si, SiO 2 , Si 3 N 4 , and WSi.
[0014]
In addition, the cleaning gas according to the present invention can be used by appropriately mixing other gases. Examples of such other gas include He, Ne, Ar, O 2 and the like. The blending amount of such other gas is not particularly limited, and can be determined in accordance with the amount, thickness, and the like of deposits attached to a chamber such as a CVD apparatus.
[0015]
The method for producing these fluorine compounds is not particularly limited. For example, CF 3 COOCHF 2 can be produced with good yield by the following method.
(CH 3 COO) 2 Hg + 2CF 2 HI → 2CH 3 COOCHF 2 + HgI The reaction temperature is 20 to 80 ° C., preferably about 40 to 70 ° C., and the reaction time is 2 to 30 hours, preferably 10 to 10 ° C. It is desirable to be about 20 hours. The reaction can be performed without a solvent.
[0016]
For example, CF 3 COOC 2 F 5 can be obtained by direct action of F 2 gas on CH 3 COOC 2 H 5 at a low temperature (−196 to 0 ° C.).
The material of the chamber using the chamber cleaning gas according to the present invention is not particularly limited, and may be a known material. Examples of such a chamber material include stainless steel, aluminum, and alloys thereof. The chamber cleaning gas according to the present invention is less likely to cause corrosion or the like on such a chamber, and can selectively and quickly remove the deposits attached to the chamber.
[0017]
In order to clean the deposits made of the silicon compound in the chamber using such a fluorine compound according to the present invention, a known method can be adopted, for example, plasma cleaning, remote plasma cleaning, microwave cleaning, etc. Various dry cleaning methods can be applied.
With such a chamber cleaning gas according to the present invention, it is possible to remove the silicon-based compound.
[Etching gas for silicon compound film]
The silicon compound film etching gas according to the present invention is at least one selected from the group consisting of CF 3 COOCHF 2 , C 2 F 5 COOCHF 2 , CF 3 COOC 2 F 5 and C 2 F 5 COOC 2 F 5. This is a fluorine-based compound.
[0018]
Among these, in the present invention, it is preferable to use CF 3 COOCHF 2 and / or C 2 F 5 COOCHF 2 as an etching gas for the silicon-based compound film.
These fluorine compounds can be used for etching alone or in combination of two or more.
[0019]
In addition, as an etching gas according to the present invention, a simple gas such as He, Ne, Ar, H 2 , N 2 , or O 2 and a compound gas such as CH 4 , C 2 H 6 , or NH 3 are appropriately mixed and used. Can do. The blending amount of such other gas is not particularly limited, and can be determined according to the thickness, amount, etc., of the silicon-based compound film that is an object to be etched.
Examples of the target compound for etching include a thin film made of a silicon-based compound. As such a silicon-based compound film, for example,
(1) a film made of silicon,
(2) At least one of oxygen, nitrogen, fluorine or carbon and a film made of silicon, or (3) a refractory metal silicite film, and the like.
[0020]
More specifically, for example, refractory metal silicite films such as Si film, SiO 2 film, Si 3 N 4 film, and WSi film can be used.
As a method of etching such a silicon-based compound film with the fluorine-based compound according to the present invention, a known method can be adopted, and various dry etching methods such as plasma etching, reactive ion etching, and microwave etching are applied. it can. Moreover, well-known etching conditions can be employ | adopted for the etching conditions of a silicon-type compound film | membrane.
[0021]
Since the etching gas according to the present invention has an ester bond, it easily hydrolyzes in the atmosphere, and since the atmospheric lifetime is short, the contribution to global warming is small and in the release of the unreacted etching gas. Environmental impact can be kept small, and exhaust gas treatment is easy.
[0022]
【The invention's effect】
Since the chamber cleaning gas according to the present invention has a small contribution to global warming, it is possible to suppress the environmental influence due to the release of the unreacted chamber cleaning gas, and the exhaust gas treatment is easy. The chamber cleaning gas has a cleaning speed comparable to that of the existing gas.
[0023]
Since the etching gas for silicon-based compound film according to the present invention has a small contribution to global warming, it is possible to suppress the environmental impact due to the release of unreacted etching gas and to facilitate the exhaust gas treatment. Moreover, it is possible to perform etching while efficiently removing the silicon-based compound and maintaining the dimensional accuracy of the semiconductor pattern with high accuracy, and the etching performance is comparable to that of the existing gas.
[0024]
【Example】
EXAMPLES Hereinafter, although this invention is demonstrated in detail based on an Example, this invention is not limited by these Examples.
[0025]
[Preparation Example 1]
[Synthesis of CF 3 COOCHF 2 ]
Into a 25 ml reaction vessel made of SUS-316 that was replaced with nitrogen and dried, the reactor was charged with 2.2 g (10 mmol) of (CF 3 COO) 2 Hg, and the reaction vessel was depressurized. After cooling with liquid nitrogen, 220 ml (9.15 mmol) of CF 2 HI was added. Next, the reaction vessel was heated to 50 ° C. and reacted at this temperature for 15.5 hours.
[0026]
The obtained compound (boiling point 19 ° C.) was analyzed by gas chromatography and FT-IR, and it was confirmed that the obtained compound was CF 3 COOCHF 2 . The yield was 99%.
[0027]
[Example 1]
[Chamber cleaning]
Silicon in which a SiO 2 film is deposited using a mixed gas containing 35% CF 3 COOCHF 2 synthesized in Preparation Example 1 and 65% oxygen under the conditions of a pressure of 110 Pa, an input Rf power of 290 W, and a total gas flow rate of 60 sccm. The wafer was placed in a CVD chamber to clean the SiO 2 film.
[0028]
When cleaned for 2 minutes under the above conditions, the cleaning rate was 540 kg / min.
[0029]
[Example 2]
[Chamber cleaning]
Using a mixed gas containing 25% CF 3 COOCHF 2 synthesized in Preparation Example 1 and 75% oxygen, a Si 3 N 4 film is deposited under conditions of pressure 110 Pa, input Rf power 290 W, and total gas flow rate 60 sccm. The silicon wafer was placed in a CVD chamber to clean the Si 3 N 4 film.
[0030]
When cleaned for 2 minutes under the above-mentioned conditions, the cleaning speed was 4850 kg / min.
[0031]
[Example 3]
[etching]
Using a mixed gas containing 45% CF 3 COOCHF 2 synthesized in Preparation Example 1 and 60% oxygen, under the conditions of pressure 110 Pa, input Rf power 300 W, total gas flow rate 60 sccm, Si 3 N 4 film, SiO 2 The silicon wafer on which the two films were deposited was etched to obtain the selectivity ratio between the Si 3 N 4 film and the SiO 2 film (Si 3 N 4 film etching rate / SiO 2 film etching rate). 17 times.
[0032]
[Comparative Example 1]
[Chamber cleaning]
Using a mixed gas containing 35% C 2 F 6 and 65% oxygen, a silicon wafer having a SiO 2 film deposited in a CVD chamber under the conditions of pressure 110 Pa, input Rf power 290 W, total gas flow 60 sccm The SiO 2 film was placed and cleaned.
[0033]
When cleaned for 2 minutes under the above conditions, the cleaning rate was 630 Å / min.
Since C 2 F 6 has a large global warming effect, it is a gas that is required to be replaced with a cleaning gas having a small effect.

Claims (8)

CF3COOCHF2、C25COOCHF2、CF3COOC25及びC25COOC25からなる群から選ばれる少なくとも1種のフッ素系化合物であることを特徴とするチャンバークリーニング用ガス。For at least one fluorine-based compound selected from the group consisting of CF 3 COOCHF 2 , C 2 F 5 COOCHF 2 , CF 3 COOC 2 F 5 and C 2 F 5 COOC 2 F 5 gas. 前記フッ素系化合物が、CF3COOCHF2またはC25COOCHF2から選ばれる少なくとも1種であることを特徴とする請求項1に記載のチャンバークリーニング用ガス。The chamber cleaning gas according to claim 1, wherein the fluorine-based compound is at least one selected from CF 3 COOCHF 2 and C 2 F 5 COOCHF 2 . 前記チャンバークリーニング用ガスが、CVD装置チャンバーのクリーニング用ガスであることを特徴とする請求項1または2に記載のチャンバークリーニング用ガス。The chamber cleaning gas according to claim 1, wherein the chamber cleaning gas is a cleaning gas for a CVD apparatus chamber. 前記チャンバークリーニング用ガスが、ケイ素系化合物からなる付着物のクリーニング用ガスであることを特徴とする請求項1〜3のいずれかに記載のチャンバークリーニング用ガス。The chamber cleaning gas according to claim 1, wherein the chamber cleaning gas is a cleaning gas for deposits made of a silicon compound. 前記ケイ素系化合物が、
(1)ケイ素からなる化合物、
(2)酸素、窒素、フッ素または炭素のうちの少なくとも1種と、ケイ素とからなる化合物、または
(3)高融点金属シリサイトからなる化合物
のうちの少なくとも1種であることを特徴とする請求項4に記載のチャンバークリーニング用ガス。
The silicon compound is
(1) a compound comprising silicon,
(2) At least one of oxygen, nitrogen, fluorine or carbon and a compound composed of silicon, or (3) at least one compound composed of a refractory metal silicite. Item 5. The chamber cleaning gas according to Item 4.
CF3COOCHF2、C25COOCHF2、CF3COOC25及びC25COOC25からなる群から選ばれる少なくとも1種のフッ素系化合物であることを特徴とするケイ素系化合物膜用エッチングガス。A silicon compound characterized by being at least one fluorine-based compound selected from the group consisting of CF 3 COOCHF 2 , C 2 F 5 COOCHF 2 , CF 3 COOC 2 F 5 and C 2 F 5 COOC 2 F 5 Etching gas for film. 前記ケイ素系化合物膜が、
(1)ケイ素からなる膜、
(2)酸素、窒素、フッ素または炭素のうちの少なくとも1種と、ケイ素とからなる膜、または
(3)高融点金属シリサイト膜
のうちの少なくとも1種であることを特徴とする請求項6に記載のケイ素系化合物膜用エッチングガス。
The silicon-based compound film is
(1) a film made of silicon,
7. (2) At least one of oxygen, nitrogen, fluorine or carbon and silicon, or (3) at least one of refractory metal silicite films. Etching gas for silicon-based compound film as described in 1.
前記フッ素系化合物が、CF3COOCHF2またはC25COOCHF2から選ばれる少なくとも1種であることを特徴とする請求項6または7に記載のケイ素系化合物膜用エッチングガス。8. The etching gas for a silicon-based compound film according to claim 6, wherein the fluorine-based compound is at least one selected from CF 3 COOCHF 2 or C 2 F 5 COOCHF 2 .
JP2000207473A 2000-07-07 2000-07-07 Cleaning gas and etching gas Expired - Lifetime JP3865113B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2000207473A JP3865113B2 (en) 2000-07-07 2000-07-07 Cleaning gas and etching gas
PCT/JP2001/005761 WO2002005338A1 (en) 2000-07-07 2001-07-03 Cleaning gas and etching gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000207473A JP3865113B2 (en) 2000-07-07 2000-07-07 Cleaning gas and etching gas

Publications (2)

Publication Number Publication Date
JP2002020796A JP2002020796A (en) 2002-01-23
JP3865113B2 true JP3865113B2 (en) 2007-01-10

Family

ID=18704228

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000207473A Expired - Lifetime JP3865113B2 (en) 2000-07-07 2000-07-07 Cleaning gas and etching gas

Country Status (2)

Country Link
JP (1) JP3865113B2 (en)
WO (1) WO2002005338A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100569541B1 (en) 2004-03-08 2006-04-10 주식회사 하이닉스반도체 Method for Manufacturing of Semiconductor Device

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06163476A (en) * 1992-11-18 1994-06-10 Sony Corp Dry etching method
US5626775A (en) * 1996-05-13 1997-05-06 Air Products And Chemicals, Inc. Plasma etch with trifluoroacetic acid and derivatives
JPH10223614A (en) * 1997-02-12 1998-08-21 Daikin Ind Ltd Etching gas and cleaning gas
JP2000038675A (en) * 1998-07-22 2000-02-08 Central Glass Co Ltd Cleaning gas

Also Published As

Publication number Publication date
JP2002020796A (en) 2002-01-23
WO2002005338A1 (en) 2002-01-17

Similar Documents

Publication Publication Date Title
JP3878972B2 (en) Gas composition for cleaning the interior of a reactor and for etching a film of a silicon-containing compound
JP4112198B2 (en) Cleaning gas and etching gas, and chamber cleaning method and etching method
US4529476A (en) Gas for selectively etching silicon nitride and process for selectively etching silicon nitride with the gas
CN104752142B (en) Regulate and control the method for plasma reaction chamber environment
CN1119385C (en) Gas for removing deposit and removal method using same
JP2002500444A (en) Etching and cleaning method using fluorinated carbonyl compound
JP5942985B2 (en) Plasma etching gas and plasma etching method
JP6952766B2 (en) Dry etching method or dry cleaning method
JP3865113B2 (en) Cleaning gas and etching gas
JP4703865B2 (en) Method for producing perfluorocarbons and use thereof
KR100562514B1 (en) Cleaning gas and etching gas
JP2004266077A (en) Method of cleaning cvd chamber and cleaning gas used therefor
JP3007032B2 (en) Gas cleaning method for tungsten and tungsten compound film forming apparatus
JP3014368B2 (en) Cleaning gas
JP2002184765A (en) Cleaning gas
JP2003218100A (en) Mixture cleaning gas composition
JP3555737B2 (en) Cleaning gas
JP3468412B2 (en) Cleaning gas
JP2000297377A (en) CLEANING METHOD FOR Si3N4 FILM FORMING DEVICE
JP2005199128A (en) Process system, exhaust gas treatment method, and glass
JPH06173012A (en) Gaseous mixed cleaning composition

Legal Events

Date Code Title Description
A711 Notification of change in applicant

Free format text: JAPANESE INTERMEDIATE CODE: A711

Effective date: 20050816

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20050816

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20060830

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20060927

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

Ref document number: 3865113

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313115

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313115

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111013

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121013

Year of fee payment: 6

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121013

Year of fee payment: 6

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121013

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131013

Year of fee payment: 7

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313117

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

EXPY Cancellation because of completion of term